Erhuma Mabruk, Köbel Martin, Mustafa Tarek, Wulfänger Jens, Dralle Henning, Hoang-Vu Cuong, Langner Jürgen, Seliger Barbara, Kehlen Astrid
Institute of Medical Immunology, Martin-Luther University Halle Wittenberg, Germany.
Int J Cancer. 2007 Jun 1;120(11):2393-400. doi: 10.1002/ijc.22252.
Neutral endopeptidase (NEP/CD10) is a cell surface zinc metalloprotease cleaving peptide bounds on the amino terminus of hydrophobic amino acids and inactivating multiple physiologically active peptides. Loss or decrease in NEP/CD10 expression have been reported in many types of malignancies, but the role of NEP/CD10 in pancreatic carcinoma has not yet been identified. Using real-time RT-PCR, flow cytometry as well as immunohistochemistry, NEP/CD10 expression was quantified in both pancreatic carcinoma cell lines and in tumor specimens obtained from patients with primary pancreatic carcinomas. Three out of 8 pancreatic carcinoma cell lines exhibit heterogeneous NEP/CD10 expression levels: PATU-8988T expressed the highest NEP/CD10 levels, whereas HUP-T4 and HUP-T3 cells showed a moderate to low NEP/CD10 expression. NEP/CD10 immunoreactivity was found in 6 of 24 pancreatic ductal adenocarcinomas, but also in 3 of 6 tissues of patients with chronic pancreatitis. NEP/CD10 expression in pancreatic tumor lesions and cell lines was not associated with tumor grading and staging. Treatment of PATU-8988T cells with the histone deacetylase inhibitors sodium butyrate and valproic acid induced an increase of NEP/CD10 expression. This was accompanied by a reduced cell proliferation rate of PATU-8988T cells, which was increased by the addition of the enzyme activity inhibitors phosphoramidon and thiorphan. Thus, NEP/CD10 is differentially expressed in pancreatic tumors and might be involved in the proliferative activity of pancreatic cancer cells. However, further studies are needed to provide more detailed information of the role of NEP/CD10 under physiological and pathophysiological conditions of the pancreas.
中性内肽酶(NEP/CD10)是一种细胞表面锌金属蛋白酶,可切割疏水性氨基酸氨基末端的肽键并使多种生理活性肽失活。在许多类型的恶性肿瘤中都有NEP/CD10表达缺失或降低的报道,但NEP/CD10在胰腺癌中的作用尚未明确。通过实时逆转录聚合酶链反应、流式细胞术以及免疫组织化学方法,对胰腺癌细胞系和原发性胰腺癌患者的肿瘤标本中的NEP/CD10表达进行了定量分析。8种胰腺癌细胞系中有3种表现出NEP/CD10表达水平的异质性:PATU-8988T细胞表达的NEP/CD10水平最高,而HUP-T4和HUP-T3细胞则表现出中度至低度的NEP/CD10表达。在24例胰腺导管腺癌中有6例检测到NEP/CD10免疫反应性,在6例慢性胰腺炎患者的组织中有3例也检测到。胰腺肿瘤病变和细胞系中的NEP/CD10表达与肿瘤分级和分期无关。用组蛋白去乙酰化酶抑制剂丁酸钠和丙戊酸处理PATU-8988T细胞可诱导NEP/CD10表达增加。这伴随着PATU-8988T细胞增殖率的降低,而添加酶活性抑制剂磷酰胺素和硫磷酰胺可使其增殖率增加。因此,NEP/CD10在胰腺肿瘤中存在差异表达,可能参与胰腺癌细胞的增殖活性。然而,需要进一步研究以提供关于NEP/CD10在胰腺生理和病理生理条件下作用的更详细信息。